FDA UDI In Commercial Distribution 🇺🇸 United States

Biomet SpinalPak / OrthoPak

DI: 00812301020195 · Model: 106130-17 · EBI, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Biomet SpinalPak / OrthoPak
Primary DI
00812301020195
Version / Model
106130-17
Catalog Number
106130-17
Company Name
EBI, LLC
Labeler DUNS
050410323
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-19
Public Version
4
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
971dcc7b-c7de-468b-bdbe-2268bf413153

Device Description

ELECTRODE COVER PATCHES

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LOF Stimulator, Bone Growth, Non-Invasive

GMDN Terms

Code Name
35463 Patient-worn bone growth electromagnetic stimulator

Identifiers

Type ID
Primary 00812301020195

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P850022 008